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Organization and reimbursement of enteral and parenteral nutrition in and outside the hospital in Belgium / Patriek Mistiaen / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2019)
Organization and reimbursement of enteral and parenteral nutrition in and outside the hospital in Belgium [printed text] / Patriek Mistiaen , Author ; Audrey Cordon, Author ; Stephan Devriese , Author ; Hilde Nevens , Author ; Lorena San Miguel , Author ; Isabelle Savoye, Author ; Koen Van Den Heede , Author . - Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre, 2019 . - 139 p. : ill., ; A4. - (KCE Reports. Health Services Research (HSR); 315C) .
ISSN : D/2019/10.273/40 : € 0,00
Languages : English (eng)
Descriptors: Classification
WB 410 Special methods of feeding
Indexation
2017-07 ; Enteral Nutrition ; Nutritional Support ; Parenteral Nutrition ; R315Contents note: GENERAL INTRODUCTION 9 -- RESEARCH OBJECTIVE 12 -- RESEARCH QUESTIONS 12 -- STRUCTURE OF THE REPORT 12 -- REFERENCES INTRODUCTION 13 -- 1 PART 1 NUTRITIONAL SUPPORT TEAMS 16 -- 1.1 BACKGROUND NUTRITIONAL SUPPORT TEAMS 16 -- 1.2 NUTRITION SUPPORT TEAMS IN BELGIUM 17 -- 1.2.1 Registration 18 -- 1.3 SYSTEMATIC REVIEW NST.20 -- 1.3.1 Method .20 -- 1.3.2 Results 25 -- 1.3.3 Discussion & conclusion 40 -- 1.4 REFERENCES PART 1 42 -- 2 PART 2: PATIENTS ON ENTERAL OR PARENTERAL NUTRITION IN BELGIUM 48 -- 2.1 INTRODUCTION 48 -- 2.2 WHICH DATA EXISTS ON ENTERAL AND PARENTERAL NUTRITION? 48 -- 2.2.1 MZG–RHM – AZV-SHA (TCT) 50 -- 2.2.2 VG-MZG – DI-RHM 52 -- 2.2.3 Nutrition Support Team (NST) registration 55 -- 2.2.4 nutrition Day 55 -- 2.2.5 IMA – AIM 55 -- 2.2.6 Royal Decree parenteral nutrition (RD 2009) 58 -- 2.3 RESULTS BY MEASURE 58 -- 2.3.1 Prevalence and ratio 58 -- 2.3.2 Duration 67 -- 2.4 DISCUSSION 72 -- 2.4.1 Prevalence and ratio 73 -- 2.4.2 Duration 73 -- 2.4.3 Gaps 74 -- 2.5 REFERENCES PART 2 74 -- 3 PART 3: COSTS OF ENTERAL AND PARENTERAL NUTRITION IN BELGIUM 75 -- 3.1 COST-EFFECTIVENESS OF ENTERAL VERSUS PN: A LITERATURE REVIEW 75 -- 3.1.1 Methods 75 -- 3.1.2 Results of the economic search strategy 77 -- 3.1.3 Conclusions and limitations 86 -- 3.2 REIMBURSEMENT AND FUNDING OF ENTERAL (EN) AND PARENTERAL (PN) NUTRITION IN BELGIUM 86 -- 3.2.1 Methods 86 -- 3.2.2 Background information on reimbursement decisions for EN and PN at home 87 -- 3.2.3 Enteral and parenteral nutrition in hospital 90 -- 3.2.4 Reimbursement for EN and PN use at home in Belgium 92 -- 3.2.5 Summary of reimbursement/funding and out of pocket patient expenses for EN and PN in Belgium 97 -- 3.2.6 Other funding related to nutrition 99 -- 3.3 COSTS IN BELGIUM 100 -- 3.3.1 Total costs for bags at hospital 100 -- 3.3.2 Home care costs 102 -- 3.3.3 Incremental Budgetary estimations 104 -- 3.4 REFERENCES PART 3 109 -- 4 GENERAL CONCLUSIONS 111 -- APPENDICES 113 Link for e-copy: https://doi.org/10.57598/R315C Format of e-copy: PDF (8,1 Mb) Record link: https://kce.docressources.info/index.php?lvl=notice_display&id=4562 Passende zorg in de laatste levensfase / Kris Van den Broeck / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2017)
Passende zorg in de laatste levensfase : Synthese [printed text] / Kris Van den Broeck, Author ; Olivier Schmitz, Author ; Isabelle Aujoulat, Author ; Patriek Mistiaen , Author ; Marie Friedel, Author ; Magali Genet, Author ; Céline Ricour, Author ; Laurence Kohn , Author ; Johan Wens, Author . - Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre, 2017 . - 21 p. : ill., ; A4. - (KCE Reports A. Health Services Research (HSR); 296AS) .
ISSN : D/2017/10.273/88 : € 0,00
Languages : Dutch (nla)
Descriptors: Indexation
2015-14 ; Advance Care Planning ; Advance Directive Adherence ; Advance Directives ; Hospice and Palliative Care Nursing ; Hospice Care ; Life Support Care ; Medical Futility ; Palliative Care ; Palliative Medicine ; R296 ; Refusal to Treat ; Terminal Care ; Terminally Ill ; Treatment Refusal ; Withholding Treatment
Classification
WB 310 Hospice care. Palliative care. Terminal careAbstract: Wat wordt in ons land beschouwd als passende zorg in de laatste levensfase? Hoe komt het dat sommige mensen deze zorg niet krijgen, en hoe kan dit worden voorkomen? Het Federaal Kenniscentrum voor de Gezondheidszorg (KCE) doorzocht de Belgische publicaties en organiseerde samen met het onderzoeksteam van UAntwerpen en de UCL een grootschalig onderzoek (waaronder een enquête) bij zorgverleners, patiënten, familieleden en vrijwilligers. Passende zorg blijkt zorg te zijn die tegemoet komt aan wat een patiënt belangrijk vindt. Het tijdig vastleggen van wensen en voorkeuren in een voorafgaande zorgplanning is een zeer goede manier om niet passende zorg bij het levenseinde te voorkomen. Daarnaast moeten zorgverleners vooral tijd krijgen en maken voor gesprekken met hun patiënt. Wat verwacht deze nog van het leven? Waar liggen de prioriteiten? En de maatschappij moet opnieuw leren om te gaan met het levenseinde, zodat dit gemakkelijker bespreekbaar wordt tussen de patiënt en zijn naasten en zorgverleners. Contents note: 1. INLEIDING 4 -- 1.1. ACHTERGROND 4 -- 2. SCOPE VAN DE STUDIE EN METHODE .. 4 -- 2.1. WAT HEBBEN WE ONDERZOCHT? 4 -- 2.2. HOE GINGEN WE TE WERK? 4 -- 2.2.1. Onderzoek van de literatuur 4 -- 2.2.2. Onderzoek met online enquête, interviews en focusgroepen 5 -- 2.2.3. Stakeholderoverleg en validatie 5 -- 3. WAT IS (NIET) PASSENDE ZORG BIJ HET LEVENSEINDE? 6 -- 3.1. VELE TERMEN EN BETEKENISSEN VOOR NIET PASSENDE ZORG 6 -- 3.2. PREVALENTIE VAN NIET PASSENDE ZORG 7 -- 4. WAT WERKT (NIET) PASSENDE ZORG IN DE HAND? 7 -- 4.1. MAATSCHAPPIJ 7 -- 4.2. ZORGORGANISATIE. 8 -- 4.3. ZORGVERLENERS 9 -- 4.4. FAMILIELEDEN 10 -- 4.5. PATIËNT 10 -- 4.5.1. Onrealistische verwachtingen en onwetendheid over palliatieve zorg 10 -- 4.5.2. Terughoudendheid 10 -- 4.5.3. Soort van aandoening 11 -- 4.5.4. Andere factoren 11 -- 5. HOE PASSENDE ZORG BEVORDEREN? 11 -- 5.1. MAATSCHAPPIJ (EN PATIËNTEN) 11 -- 5.2. ZORGORGANISATIE 12 -- 5.3. ZORGVERLENERS 13 -- 6. CONCLUSIE. 15 Link for e-copy: https://doi.org/10.57598/R296AS Format of e-copy: PDF (429 Kb) Record link: https://kce.docressources.info/index.php?lvl=notice_display&id=4347 Position du KCE concernant l’implication des patients dans les projets de recherche en politique des soins de santé / Irina Cleemput / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2019)
Position du KCE concernant l’implication des patients dans les projets de recherche en politique des soins de santé : Synthèse [printed text] / Irina Cleemput , Author ; Marie Dauvrin , Author ; Laurence Kohn , Author ; Patriek Mistiaen , Author ; Wendy Christiaens , Author ; Christian Léonard , Author . - Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre, 2019 . - 22 p. : ill., ; A4. - (KCE Reports B. Method; 320Bs) .
ISSN : D/2019/10.273/55 : € 0,00
Languages : French (fre)
Descriptors: Classification
W 84.3 Health Services Research (General)
Indexation
2018-72 ; Methods ; Patient Participation ; Policy ; R320 ; ResearchAbstract: C’est une tendance mondiale depuis cinq à dix ans : les patients sont de plus en plus souvent impliqués dans la recherche scientifique lorsqu’elle vise à conseiller les décideurs politiques sur les orientations en matière de soins de santé. Cependant, cela se produit encore trop souvent ‘parce qu’il le faut bien’ et leurs connaissances spécifiques en tant qu'experts du vécu ne sont pas suffisamment prises en compte. Le Centre fédéral d’Expertise en Soins de Santé (KCE) est la première institution publique belge à examiner comment elle peut impliquer les patients de la manière la plus structurelle et la plus cohérente possible dans ses études. Il formule 18 prises de position sur le sujet, la prochaine étape étant l’élaboration d’un guide méthodologique proposant des recommandations pratiques. Contents note: PRÉFACE 1 -- SYNTHÈSE 2 -- 1. CONTEXTE 4 -- 1.1. UN PROCESSUS AXE EN PREMIERE INSTANCE SUR DES APPROCHES QUANTITATIVES 4 -- 1.2. OBJECTIF ET APPROCHE DE CETTE ETUDE 4 -- 2. QU’ENTEND-ON PAR « IMPLICATION DES PATIENTS » ? 5 -- 2.1. LE ROYAUME-UNI PIONNIER 5 -- 2.2. IMPLICATION POUR CERTAINES PHASES DE LA RECHERCHE, OU POUR TOUTES 5 -- 2.3. PLUSIEURS NIVEAUX D’IMPLICATION 6 -- 3. QUI EST « LE PATIENT » ? 7 -- 4. POURQUOI IMPLIQUER LES PATIENTS DANS LA RECHERCHE À VISÉE POLITIQUE ? 8 -- 4.1. MOTIFS ETHIQUES ET PHILOSOPHIQUES FONDAMENTAUX 8 -- 4.2. MOTIFS PROCEDURAUX ET INSTRUMENTAUX 8 -- 5. EFFETS ET DÉFIS DE L’IMPLICATION DES PATIENTS DANS LA RECHERCHE 9 -- 5.1. EFFETS POSITIFS 9 -- 5.2. DEFIS 10 -- 6. CONDITIONS ET FACTEURS DE RÉUSSITE DE L’IMPLICATION DES PATIENTS DANS LA RECHERCHE 11 -- 6.1. QUAND L’IMPLICATION DES PATIENTS A-T-ELLE UN SENS ? 11 -- 6.2. CONDITIONS ET FACTEURS DE REUSSITE 12 -- 7. LE KCE EST-IL OUVERT À UNE IMPLICATION ACCRUE DES PATIENTS ? 14 -- 7.1. LA CULTURE INTERNE DU KCE 14 -- 7.2. UNE MAJORITE D’ARGUMENTS « POUR » 14 -- 8. QUELS PATIENTS LE KCE VEUT-IL IMPLIQUER DANS SES ÉTUDES, QUAND ET POURQUOI ? 15 -- 8.1. LE ROLE DES PATIENTS AU KCE NE CESSE DE SE DEVELOPPER 15 -- 8.2. QUELS PATIENTS IMPLIQUER ? 16 -- 8.3. LE KCE PARTISAN D’UNE CONCERTATION INTEGREE… 16 -- 8.4. … SOUS CERTAINES CONDITIONS 16 -- 9. POSITIONS DU KCE 17 -- RÉFÉRENCES 19 Link for e-copy: https://doi.org/10.57598/R320BS Format of e-copy: PDF (0,8 Mb) Record link: https://kce.docressources.info/index.php?lvl=notice_display&id=4617 Position of KCE on patient involvement in health care policy research / Irina Cleemput / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2019)
Position of KCE on patient involvement in health care policy research [printed text] / Irina Cleemput , Author ; Marie Dauvrin , Author ; Laurence Kohn , Author ; Patriek Mistiaen , Author ; Wendy Christiaens , Author ; Christian Léonard , Author . - Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre, 2019 . - 240 p. : ill., ; A4. - (KCE Reports. Method; 320) .
ISSN : D/2019/10.273/57 : € 0,00
Languages : English (eng)
Descriptors: Classification
W 84.3 Health Services Research (General)
Indexation
2018-72 ; Methods ; Patient Participation ; Policy ; R320 ; ResearchContents note: SCIENTIFIC REPORT 16 -- 1 BACKGROUND AND SCOPE 16 -- 2 DEFINITIONS 18 -- 2.1 INVOLVEMENT, ENGAGEMENT, PARTICIPATION 18 -- 2.2 PATIENTS, PATIENT REPRESENTATIVES, CAREGIVERS ETC 21 -- 2.3 PATIENT INVOLVEMENT VERSUS QUALITATIVE RESEARCH ABOUT PATIENT-RELATED ISSUES 22 -- 3 RATIONALES FOR PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH 24 -- 3.1 REASONS FOR INVOLVING PATIENTS IN POLICY RESEARCH 24 -- 3.2 GOALS OF PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH 26 -- 4 PHILOSOPHICAL AND ANTHROPOLOGICAL REASONS FOR TAKING THE PATIENT VOICE INTO CONSIDERATION IN HEALTHCARE RESEARCH 28 -- 4.1 FREEDOM, RESPONSIBILITY AND MERIT 28 -- 4.2 THE NORMAL AND THE PATHOLOGICAL 31 -- 4.3 RECOVERY AND IMPROVEMENT 33 -- 4.4 CONCLUDING REMARKS 35 -- 5 WHEN TO INVOLVE PATIENTS IN A RESEARCH PROJECT 35 -- 5.1 IDENTIFICATION AND PRIORITIZATION OF RESEARCH TOPICS 36 -- 5.2 DEFINING THE PROBLEM, SCOPE, OBJECTIVES AND DESIGN OF THE STUDY 38 -- 5.3 ASSESSMENT OF SCIENTIFIC LITERATURE AND OTHER SOURCES OF INFORMATION, DATA COLLECTION AND DATA ANALYSIS 39 -- 5.4 REPORTING THE RESULTS OF THE STUDY 40 -- 5.5 FORMULATION OF RECOMMENDATIONS 40 -- 5.6 DISSEMINATION 41 -- 6 HOW TO SELECT PATIENTS TO BE INVOLVED? 43 -- 6.1 IDENTIFICATION 43 -- 6.2 RECRUITMENT 44 -- 7 BENEFITS, RISKS AND CHALLENGES OF PATIENT INVOLVEMENT IN RESEARCH 47 -- 7.1 BENEFITS, RISKS AND CHALLENGES OF PATIENT INVOLVEMENT IN RESEARCH: FINDINGS OF PUBLISHED LITERATURE REVIEWS 48 -- 7.2 IMPACT ON PATIENTS INVOLVED IN RESEARCH 48 -- 7.3 IMPACT ON RESEARCHERS 48 -- 7.4 IMPACT ON RESEARCH PROCESSES AND OUTCOMES 49 -- 7.5 HOW TO ASSESS THE IMPACT OF PATIENT INVOLVEMENT IN RESEARCH? 52 -- 8 STANDARDS FOR PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH 53 -- 8.1 GENERAL REQUIREMENTS FOR MEANINGFUL PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH 53 -- 8.1.1 Culture 53 -- 8.1.2 Leadership and coordination 54 -- 8.1.3 Economic resources 54 -- 8.1.4 Information and training 54 -- 8.2 GUIDANCE FROM LITERATURE 55 -- 8.3 INVOLVE’S NATIONAL STANDARDS FOR PUBLIC INVOLVEMENT IN RESEARCH 57 -- 8.4 HTAI’S QUALITY STANDARDS FOR PATIENT INVOLVEMENT IN HEALTH TECHNOLOGY ASSESSMENT 59 -- 8.5 GOOD CLINICAL PRACTICE GUIDELINES 60 -- 8.6 TRIALS 62 -- 8.7 COMMUNITY-BASED PARTICIPATORY RESEARCH 64 -- 9 ORGANISATION AND GOVERNANCE OF PATIENT INVOLVEMENT 65 -- 9.1 LITERATURE 65 -- 9.2 PATIENTS AS STRUCTURAL MEMBERS OF ADVISORY COMMITTEES, BOARDS OR COUNCILS 66 -- 9.2.1 German Federal Joint Committee (G-BA) 66 -- 9.2.2 National Institute for Health and Care Excellence (NICE) 67 -- 9.2.3 Canadian Agency for Drugs and Technologies in Health 68 -- 9.3 PATIENTS AS ADVISORS 69 -- 9.3.1 Examples from the Netherlands 69 -- 9.3.2 National Institute for Health and Care Excellence (NICE) 70 -- 9.3.3 Healthcare Improvement Scotland 71 -- 9.3.4 Canadian Agency for Drugs and Technologies in Health 72 -- 10 PATIENT INVOLVEMENT IN INTERNATIONAL NETWORKS AND ORGANISATIONS 73 -- 10.1 EUNETHTA 73 -- 10.1.1 Patient involvement in early dialogues 73 -- 10.1.2 Patient involvement in joint and collaborative HTAs 74 -- 10.1.3 Eligibility rules for patients and consumers 74 -- 10.1.4 Experience with patient and consumer involvement so far 75 -- 10.2 REDETS 75 -- 10.2.1 Concepts 76 -- 10.2.2 Principles 76 -- 10.2.3 Levels of involvement 78 -- 10.2.4 Design and procedures 78 -- 10.2.5 Patient selection and recruitment 80 -- 10.2.6 Recommendations: short term, medium term, long term 81 -- 10.3 EUROPEAN MEDICINES AGENCY 85 -- 10.3.1 Objectives of patient involvement at EMA 85 -- 10.3.2 Who to involve? 86 -- 10.3.3 Experience with patient involvement 88 -- 10.3.4 Future plans 88 -- 10.4 FOOD AND DRUG ADMINISTRATION 89 -- 10.4.1 Objectives of patient involvement at the FDA 89 -- 10.4.2 Who to involve? 90 -- 10.4.3 Experience with patient involvement 91 -- 11 EMBEDDED PATIENT INVOLVEMENT PROGRAMMES AND INITIATIVES 92 -- 11.1 JAMES LIND ALLIANCE 92 -- 11.2 INVOLVE 93 -- 11.3 PCORI 94 -- 11.4 SPOR 95 -- 11.5 EUPATI 95 -- 11.6 OTHER INITIATIVES: PFMD, PARTICIPATIEKOMPAS, PARADIGM 95 -- 12 PATIENT INVOLVEMENT EXPERIENCES IN BELGIUM 96 -- 12.1 OVERVIEW OF THE PROCESS AND GENERAL TIMELINES 97 -- 12.2 SELECTION AND RECRUITMENT OF THE PARTICIPANTS 97 -- 12.2.1 Researchers 97 -- 12.2.2 Funding agencies 98 -- 12.2.3 Patient representatives 99 -- 12.2.4 Sickness funds 99 -- 12.3 DATA COLLECTION 99 -- 12.4 DATA ANALYSIS 99 -- 12.5 EXPERIENCES OF THE BELGIAN RESEARCH CENTRES 99 -- 12.5.1 Description of the sample 99 -- 12.5.2 Institute of Tropical Medicine: Community-based participatory research project 100 -- 12.5.3 ULiège: patients involved in different roles 100 -- 12.5.4 UCLouvain & Haute Ecole Léonard de Vinci: Participate Brussels 101 -- 12.5.5 Observatoire du sida et des sexualités : patients as initiators, co-researchers and research leaders 102 -- 12.5.6 Institut Jules Bordet: patients involved in the design of clinical trials 103 -- 12.5.7 Groupe Jolimont: patient partner 104 -- 12.5.8 UGent: longstanding expertise 105 -- 12.5.9 Plateforme pour l’Amélioration de la Qualité et de Sécurité des Soins (PAQS) 105 -- 12.5.10 KU Leuven: first steps of patient involvement 106 -- 12.5.11 LiCalab, Care Living Lab for innovation in health and care 107 -- 12.5.12 ULB: patient as partner 108 -- 12.6 PATIENT REPRESENTATIVES AND PATIENTS INVOLVED IN RESEARCH 109 -- 12.6.1 Ligue des Usagers des Services de Santé (LUSS) 109 -- 12.6.2 Vlaams Patiëntenplatform (VPP) 109 -- 12.6.3 Patienten Rat und Treff (PRT) 110 -- 12.6.4 EUPATI Belgium: patients as experts 111 -- 12.6.5 ULB: patient-partner, the perspective of the patient 112 -- 12.6.6 Plateforme Prévention SIDA: patients as initiators of research 113 -- 12.7 SICKNESS FUNDS 113 -- 12.8 FUNDING AGENCIES 114 -- 12.8.1 Innoviris –Brussels region 114 -- 12.8.2 FWO - Research Foundation-Flanders 114 -- 12.8.3 F.R.S.-FNRS- Research Foundation Fédération Wallonie-Bruxelles 115 -- 12.8.4 King Baudouin Foundation (KBF) 117 -- 12.9 LESSONS LEARNT: CONSENSUS 118 -- 12.9.1 Patient involvement needs to make sense 118 -- 12.9.2 Patient involvement needs to be prepared 119 -- 12.9.3 Patient involvement takes time 120 -- 12.10 DIVERGING ISSUES 120 -- 12.10.1 Who should be included as patients? 120 -- 12.10.2 Which topics should be investigated? 122 -- 12.10.3 Should the patient be paid? 123 -- 12.10.4 In which stages of the research should the patient be involved? 123 -- 12.11 ENABLERS OF PARTICIPATION 124 -- 12.11.1 Supporting organisational and legal context 124 -- 12.11.2 Relational aspects 125 -- 12.11.3 Valorisation of the patients ‘contribution 125 -- 12.11.4 Preparation of researchers 125 -- 12.11.5 Definition of the role of researchers 125 -- 12.11.6 Definition of the roles of patients 126 -- 12.12 BARRIERS TO PARTICIPATION 126 -- 12.13 SUMMARY OF LESSONS LEARNT FROM BELGIAN PATIENT INVOLVEMENT EXPERIENCES 127 -- 13 PATIENT INVOLVEMENT CULTURE AT KCE 128 -- 13.1 METHOD: KCE’S “PATIENTS-ON-BOARD”-GAME 128 -- 13.1.1 Objectives of the game 129 -- 13.1.2 Organization 129 -- 13.1.3 Data analysis 129 -- 13.2 RESULTS 130 -- 13.2.1 Quantitative exploration 130 -- 13.2.2 Qualitative findings 132 -- 13.3 CONCLUSION WITH RESPECT TO THE ACTUAL PATIENT INVOLVEMENT CULTURE AT KCE 139 -- 14 THE CURRENT PLACE OF PATIENT INVOLVEMENT IN KCE PROJECTS 140 -- 14.1 PATIENT INVOLVEMENT IN DEFINING HEALTH POLICY 140 -- 14.2 PATIENT INVOLVEMENT IN THE DEVELOPMENT OF A TOOL FOR SHARED DECISION MAKING 141 -- 14.3 PATIENT INVOLVEMENT IN THE DIFFERENT DOMAINS OF KCE RESEARCH 141 -- 14.4 METHODOLOGICAL REPORTS USEFUL TO INVOLVE PATIENTS 142 -- 14.5 INVOLVEMENT OF PATIENTS IN RECENT KCE RESEARCH 142 -- 14.5.1 Methods 142 -- 14.5.2 Results 143 -- 14.5.3 Conclusions 146 -- 15 FORMULATION OF POSITION STATEMENTS 147 -- 15.1 GENERAL APPROACH 147 -- 15.2 FIRST DRAFT STATEMENTS 147 -- 15.3 ASSESSMENT OF THE SUPPORT FOR THE STATEMENTS BY THE KCE MEMBERS 149 -- 15.3.1 Method 149 -- 15.3.2 Results 150 -- 16 KCE’S POSITION STATEMENTS REGARDING PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH 162 -- APPENDICES 164 -- APPENDIX 1. LITERATURE SEARCH AND CLASSIFICATION 164 -- APPENDIX 1.1. INTRODUCTION 164 -- APPENDIX 1.2. SOURCES 164 -- APPENDIX 1.2.1. PUBMED 164 -- APPENDIX 1.2.2. GOOGLE 165 -- APPENDIX 1.2.3. WEBSITES 165 -- APPENDIX 1.2.4. CITING SEARCH 166 -- APPENDIX 1.3. INCLUSION CRITERIA 166 -- APPENDIX 1.4. CLASSIFICATION OF RETAINED PAPERS 166 -- APPENDIX 1.4.1. REFERENCES RELATED TO DEFINITIONS AND TERMINOLOGY IN PATIENT INVOLVEMENT 166 -- APPENDIX 1.4.2. REFERENCES RELATED TO RATIONALE FOR PATIENT INVOLVEMENT 169 -- APPENDIX 1.4.3. REFERENCES RELATED TO METHODS FOR PATIENT INVOLVEMENT 173 -- APPENDIX 1.4.4. REFERENCES RELATED TO EFFECTS OF PATIENT INVOLVEMENT 179 -- APPENDIX 1.5. SUMMARY OF FINDINGS FROM REVIEWS ON THE APPLICATION, BENEFITS, RISKS AND CHALLENGES OF PATIENT INVOLVEMENT IN RESEARCH 184 -- APPENDIX 2. EXAMPLES OF PATIENT INVOLVEMENT STRUCTURES IN HTA AGENCIES 192 -- APPENDIX 2.1. NATIONAL INSTITUTE FOR HEALTH AND CARE EXCELLENCE (NICE) 192 -- APPENDIX 2.1.1. RATIONALE AND OBJECTIVES FOR PATIENT AND PUBLIC INVOLVEMENT 192 -- APPENDIX 2.1.2. NICE’S PUBLIC INVOLVEMENT POLICY 192 -- APPENDIX 2.1.3. ORGANIZATION AND COORDINATION OF PATIENT INVOLVEMENT ACTIVITIES 193 -- APPENDIX 2.1.4. EXPERIENCE WITH PATIENT INVOLVEMENT AND EVALUATION 193 -- APPENDIX 2.2. HEALTHCARE IMPROVEMENT SCOTLAND 195 -- APPENDIX 2.3. CANADIAN AGENCY FOR DRUGS AND TECHNOLOGIES IN HEALTH 196 -- APPENDIX 3. INTERVIEW GUIDES FOR THE SEMI-STRUCTURED INTERVIEWS ABOUT PROJECTS INVOLVING PATIENTS 197 -- APPENDIX 3.1. INTERVIEW GUIDE FOR RESEARCH CENTRES 197 -- APPENDIX 3.2. INTERVIEW GUIDE FOR SICKNESS FUNDS 198 -- APPENDIX 4. KCE CULTURE DATA ANALYSIS 199 -- APPENDIX 4.1. OVERARCHING THEMES AND CORRESPONDING NODES 199 -- APPENDIX 4.2. FULL LIST OF ARGUMENTS FOR OR AGAINST PATIENT INVOLVEMENT AND CONDITIONS FOR PATIENT INVOLVEMENT IN DIFFERENT PHASES OF THE RESEARCH PROCESS, ACCORDING TO OVERARCHING THEMES 204 -- APPENDIX 5. QUESTIONNAIRE ABOUT PAST AND ONGOING PATIENT INVOLVEMENT ACTIVITIES AT KCE 213 -- APPENDIX 6. SUPPORT OF POSITION STATEMENTS BY KCE EMPLOYEES 224 -- APPENDIX 6.1. RESULTS OF THE FIRST VOTING ROUND OF THE DELPHI PROCESS 224 -- APPENDIX 6.2. RESULTS OF THE SECOND VOTING ROUND OF THE DELPHI PROCESS 226 -- REFERENCES 227 Link for e-copy: https://doi.org/10.57598/R320C Format of e-copy: PDF (6,2 Mb) Record link: https://kce.docressources.info/index.php?lvl=notice_display&id=4615 Position of KCE on patient involvement in health care policy research / Irina Cleemput / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2019)
Position of KCE on patient involvement in health care policy research : Short Report [printed text] / Irina Cleemput , Author ; Marie Dauvrin , Author ; Laurence Kohn , Author ; Patriek Mistiaen , Author ; Wendy Christiaens , Author ; Christian Léonard , Author . - Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre, 2019 . - 22 p. : ill., ; A4. - (KCE Reports. Method; 320Cs) .
€ 0,00
Languages : English (eng)
Descriptors: Classification
W 84.3 Health Services Research (General)
Indexation
2018-72 ; Methods ; Patient Participation ; Policy ; R320 ; ResearchContents note: SHORT REPORT 1 -- 1. BACKGROUND 4 -- 2. WHAT IS PATIENT INVOLVEMENT 5 -- 2.1. DEFINITION 5 -- 2.2. INVOLVEMENT IN ALL OR SOME RESEARCH PHASES 5 -- 2.3. DIFFERENT LEVELS OF INVOLVEMENT 5 -- 3. WHO IS “THE PATIENT”? 6 -- 4. WHAT IS THE RATIONALE FOR INVOLVING PATIENTS IN POLICY RESEARCH? 7 -- 4.1. FUNDAMENTAL ETHICAL RATIONALES 7 -- 4.2. PROCEDURAL AND INSTRUMENTAL RATIONALES 7 -- 5. WHAT ARE THE EFFECTS OF PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH 9 -- 5.1. POSITIVE EFFECTS 9 -- 5.2. BARRIERS, RISKS AND CHALLENGES .10 -- 6. REQUIREMENTS FOR MEANINGFUL PATIENT INVOLVEMENT IN RESEARCH 11 -- 6.1. WHEN DOES PATIENT INVOLVEMENT MAKE SENSE? 11 -- 6.2. STANDARDS FOR PATIENT INVOLVEMENT 12 -- 7. IS KCE READY FOR PATIENT INVOLVEMENT? .13 -- 7.1. KCE CULTURE 13 -- 7.2. MORE ARGUMENTS PRO THAN CONTRA PATIENT INVOLVEMENT .14 -- 8. WHO, WHEN AND FOR WHAT? .15 -- 8.1. INCREASING ROLE OF PATIENTS AT KCE .15 -- 8.2. WHO TO INVOLVE AND WHEN? 15 -- 8.3. EMBEDDED CONSULTATION 16 -- 8.4. … UNDER SPECIFIC CONDITIONS 16 -- 8.5. COMMITMENT TOWARDS THE PATIENTS INVOLVED 16 -- 9. KCE’S POSITION STATEMENTS REGARDING PATIENT INVOLVEMENT IN HEALTH POLICY RESEARCH .17 -- REFERENCES 19 Link for e-copy: https://doi.org/10.57598/R320CS Format of e-copy: PDF (0,8 Mb) Record link: https://kce.docressources.info/index.php?lvl=notice_display&id=4616 Pour une réforme des soins de santé en Prison / Marie Dauvrin / Brussel [BE] : Fédération des maisons médicales et collectifs de santé francophones (2018)
PermalinkProposals for a further expansion of day surgery in Belgium / Roos Leroy / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2017)
PermalinkProposals for a further expansion of day surgery in Belgium / Roos Leroy / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2017)
PermalinkProposals for a further expansion of day surgery in Belgium / Roos Leroy / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2017)
PermalinkProposals for a further expansion of day surgery in Belgium / Roos Leroy / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2017)
PermalinkDe qui et de quoi parlons-nous / Marie Dauvrin / Brussel [BE] : Fédération des maisons médicales et collectifs de santé francophones (2018)
PermalinkReduction of the treatment gap for problematic alcohol use in Belgium / Patriek Mistiaen / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2015)
PermalinkReduction of the treatment gap for problematic alcohol use in Belgium / Patriek Mistiaen / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2015)
PermalinkReduction of the treatment gap for problematic alcohol use in Belgium / Patriek Mistiaen / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2015)
PermalinkRemote monitoring of patients with COVID-19 / Justien Cornelis / Brussels [Belgium] : KCE = Federaal Kenniscentrum voor de Gezondheidszorg = Centre Fédéral d'Expertise des Soins de Santé = Belgian Health Care Knowledge Centre (2022)
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